WO2016062874A1

WO2016062874A1 - Oral administration compositions comprising an ob-fold protein variant

Info

Publication number: WO2016062874A1
Application number: PCT/EP2015/074644
Authority: WO
Inventors: Olivier KITTEN
Original assignee: Affilogic
Priority date: 2014-10-24
Filing date: 2015-10-23
Publication date: 2016-04-28
Also published as: JP2017534620A; CN106999544A; US20180085427A1; FR3027521B1; EP3209318A1; EP3209318B1; US10293025B2; FR3027521A1; CA2965765C; CA2965765A1; ES2797048T3

Abstract

The invention relates to an oral administration composition containing an OB-fold protein variant, and to the method for preparing the same.

Description

COMPOSITIONS FOR ORAL ADMINISTRATION COMPRISING A VARIANT OF A PLI-OB PROTEIN

The invention relates to the field of the preparation of oral compositions for therapeutic use, containing active ingredients that bind to targets of interest.

There are a number of diseases of the gastrointestinal system. In order to treat these diseases, it is desirable to have compositions acting directly at the site of the disease.

To do this, it is possible to develop compositions rectally, but the oral compositions are preferred by patients and allow better compliance with the treatment. Moreover, and even for treating systemic diseases (not located in the gastrointestinal system), oral administration is preferred, as far as possible to other modes of administration (and especially injections), which may request the involvement of caregivers.

Whatever the disease, there is usually a target of therapeutic interest on which the drugs are active. It can be a cellular receptor, or a surface protein of a microorganism. In general, it appears desirable to have compositions for the application of active principles acting on targets of therapeutic interest directly on the place of action. However, some proteins, such as antibodies, are degraded during passage into the stomach. The application WO 2007/139397 describes the use of OB-fold protein libraries in which the OB domain is modified by the introduction of mutations in this binding domain of the protein to its natural ligand.

The application WO 2008/068637 describes the use of a library based on the Sac7d protein to obtain ligands having an affinity for targets of interest. The method described in WO 2008/068637 comprises the generation of combinatorial libraries containing a plurality of DNA molecules having all the same sequence, except the presence of certain random mutations leading to the production of variants of a wild-type protein, having mutations to certain amino acids of the binding site of this wild-fold protein OB. In particular, in the context of WO 2008/068637, the wild-type fold-OB protein is a Sac7d protein, into which mutations are introduced to generate variability, in particular to the amino acids chosen from K7, Y8, K9, K21, K22, W24, V26, M29, S31, T33, T40, R42, A44, S46, or on other amino acids, such as V26, G27, K28, M29, S31, R42, A44, S46, E47 and K48. These amino acids are based on the sequence of Sac7d, as represented by SEQ ID No. 1.

The patent application WO 2012/150314 presents the portability of mutations of a protein of the Sac7d family to another protein of the same family. This portability amounts to creating a mutant of another protein of the Sac7d family from a mutant of a protein of said family, which has been obtained in particular by implementing the method of WO 2008/068637.

The Sac7d family is defined as pertaining to the Sac7d family and corresponds to a family of 7 kDa DNA-binding proteins isolated from extremophilic bacteria. These proteins and this family are described in particular in WO 2008/068637. Thus, in the context of the present invention, a protein belongs to the Sac7d family when it has a sequence corresponding to the sequence SEQ ID No. 8. This family comprises in particular the Sac7d or Sac7e proteins derived from Sulfolobus acidocaldarius, Sso7d resulting from Sulfolobus solfataricus, DBP 7 from Sulfolobus tokodaii, Ssh7b from Sulfolobus shibatae, Ssh7a from Sulfolobus shibatae, and p7ss from Sulfolobus solfataricus.

OB-fold proteins are known in the art. They are notably described in the documents cited above, as well as in Arcus (Curr Opin Struct Biol 2002 Dec, 12 (6): 794-801). The fold-OB is in the form of a cylinder having five beta sheets (β). Most fold-OB proteins utilize the same binding interface of their natural ligand, which may be an oligosaccharide, an oligonucleotide, a protein, a metal ion or a catalytic substrate. This binding interface mainly includes the residues located in the beta sheets. Some residues located in the loops may also be involved in the binding of a fold-OB protein with its natural ligand. Thus, the applications WO 2007/139397 and WO 2008/068637 and the document Arcus (2002, op cit) describe the binding domains of the fold-OB proteins with their natural ligand. Thus, WO 2008/068637 describes precisely how to identify the binding domain of a fold-OB protein.

By overlaying multiple sequences and 3D structures of proteins with fold-OB domains using the WU-Blast2 websites (http://www.ebi.ac.uk/blast2/index.html) (Lopez et al., 2003, Nucleic Acids Res 31, 3795-3798), T-COFFEE (http: //www.ch.embnet .org / software / TCoffee.html) (Notredame et al., 2000, J Mol Biol 302, 205-217) and DALI lite (http://www.ebi.ac.uk/DaliLite/) (Holm and Park, 2000, Bioinformatics 16, 566-567) one can identify the positions of the binding domains and in particular the amino acids that can be modified. Taking as a reference the sequence of Sac7d (SEQ ID No. 1), these residues are V2, K3, K5, K7, Y8, K9, G10, E1, K13, E14, T17, K21, K22, W24. , V26, G27, K28, M29, S31, T33, Y34, D36, N37, G38, K39, T40, R42, A44, S46, E47, K48, D49, A50 and P51.

Still with this sequence Sac7d as a reference, the residues that can be deleted are: A59, R60, A61, E64 and / or K66.

Identification of the binding domains of other fold-OB proteins can be performed as described in WO 2008/068637. This application describes that one can perform a superposition of 3D protein structures or fold-OB domains (10 domains were used in this application, including Sac7d), using the DALI website (http: //www.ebi .ac.uk / dali / Interactive.html) (Holm and Sander, 1998, Nucleic Acids Res 26, 316-319). Thus, it is easy to identify, for any protein (or any domain) with fold-OB, the amino acids involved in the binding site and corresponding to the amino acids of Sac7d mentioned above.

The teaching of WO 2008/068637 also indicates that it is optionally possible to insert amino acids in the loops of the OB-fold proteins, in particular the proteins of the Sac7d family, in particular insertions of 1 to 15 acid residues. Amines can be made in loop 3 (as defined in FIGS. 1b and 2 of WO 2008/068637), for example in the region of residues 25 to 30 of Sac7d, preferably between residues 27 and 28, insertions from 1 to 15 amino acid residues can be made in loop 4 (as defined in FIGS. 1b and 2 of WO 2008/068637), for example in the region of residues 35-40 of Sac7d, preferably between residues 37 and 38, and insertions of 1 to 20 residues can be made in loop 1 (as defined in FIGS. 1 b and 2 of WO 2008/068637), for example in the region of residues 7 to 12 of Sac7d, preferably between residues 9 and 10.

By extension, in the context of the present application, the term "fold-OB protein" comprises the natural fold-OB proteins, but also the OB-fold domains that can be isolated from more complex proteins. These fold-OB domains are described in more detail in the WO applications. 2007/139397 and WO 2008/068637. This term also includes polypeptides that can be obtained by recombinantly fusing N- or C-terminal, fold-OB protein, or OB-fold domain to a protein or a domain of interest. for example a label allowing a better purification.

The advantage of the method described in WO 2008/068637 is that it makes it possible to obtain fold-OB protein variants by screening combinatorial libraries containing or expressing a plurality of variants in which a number of amino acids have have been "randomized", that is replaced by a random amino acid. Screening of these libraries makes it possible to identify variants of these proteins that bind in a specific manner, generally with a high affinity (the application WO 2008/068637 describes indeed affinities of the order of nanomolar), with a target of interest, different from the natural ligand of the wild-type protein from which the combinatorial library was generated.

The inventors have shown that fold-OB proteins are sufficiently resistant to gastric degradation, and can remain in the intestine or cross the gut barrier and thus be used in orally usable compositions for the treatment of various diseases, especially localized at the level of the intestine, or in other organs of the body, after passage in the systemic circulation. A variant of a fold-OB protein, which binds to a target of interest, is preferably used, said target of interest being involved in a pathology, in particular of the gastrointestinal system or a systemic pathology ( that is, a pathology localized in an organ other than the gastrointestinal system).

The present invention thus relates to a composition for oral administration comprising a fold-OB protein or a wild-fold OB-protein variant, said variant having between 5 and 32 mutated residues in the binding interface. said wild-fold protein OB to its natural ligand.

In a particular embodiment, said variant has a therapeutic activity. In particular, said variant binds specifically to a target of interest different from the target of said natural ligand. This variant may then have been identified by the implementation of a method as described in WO 2008/068637 or WO 2007/139397. In fact, the implementation of the methods described in these two patent applications generally makes it possible to identify variants of any fold-OB protein binding to any target of interest. This composition also generally contains an excipient which can be used for such oral administration, and which is pharmaceutically acceptable.

As seen above, said fold-OB wild-type protein also encompasses fold-OB domains. In a preferred manner, the variant used in the context of the present invention contains at most 300 amino acids, preferably at most 200 amino acids, preferably at most 175 amino acids, more preferably at most 150 amino acids. more preferably at most 100 amino acids. In a particular embodiment, it contains at most 80 or at most 70 amino acids.

The number of residues mutated in said variant (relative to the wild-type protein) is between 5 and 32. In other embodiments, these variants preferably have at least 5, more preferably at least 8, so still more preferred at least 10, but generally less than 32, more preferably less than 24, more preferably less than 20 or less than 15 substituted amino acids relative to the OB-fold protein (or domain) wild. It is preferred when 8, 9, 10, 11, 12, 13 or 14 amino acids are mutated relative to the wild-type protein. These mutated amino acids are located in the binding site of the fold-OB protein with its natural ligand. They are generally distributed over the whole of this link domain. Given the structure of this binding domain, some mutated residues are found in one (usually several, notably two or three) beta sheets.

In a particular embodiment, these variants may also comprise amino acid insertions in loops connecting the beta sheets of the OB-fold. Thus, it is possible to introduce between 1 and 15 amino acids in the loop 1 and / or in the loop 4 and / or in the loop 3 (the loops being numbered in the same way as in WO 2008/068637.

In a particular embodiment, said wild-fold protein OB is chosen from Sac7d or Sac7e from Sulfolobus acidocaldarius, Sso7d from Sulfolobus solfataricus, DBP 7 from Sulfolobus tokodaii, Ssh7b from Sulfolobus shibatae, Ssh7a from Sulfolobus shibatae, and p7ss from Sulfolobus solfataricus.

It is therefore the protein to which is compared the variant used in the composition for oral administration of the present invention. The different sequences of Sac7d, Sso7d, Sac7e, Ssh7b, SSh7a, DBP7 and Sis7 proteins are represented by SEQ ID No. 1 to SEQ ID No. 7 respectively.

A variant of a protein of this Sac7d family is called a nanofitin. The implementation of the invention is thus preferably on variants of the proteins represented by SEQ ID No. 1 to SEQ ID No. 7, in particular on Sac7d variants.

In the case of a liquid composition, the concentration of the variant in the composition according to the present invention is generally greater than 10 ng / ml and less than 600 mg / ml. It is therefore generally less than 500 mg / ml, preferably less than 250 mg / ml, preferably less than 100 mg / ml, or 50 mg / ml, or even less than 10 mg / ml. It is generally greater than 10 ng / ml, preferably greater than 50 ng / ml, preferably greater than 100 ng / ml.

The concentration is adapted to the dose that it is desired to administer to the patient for a dose of between 5 and 20 ml.

For a solid composition, the dose is adapted according to the number of tablets (or tablets or other) that will take the patient to obtain the therapeutically effective dose.

In general, the patient is administered a very variable amount (which will depend in particular on the nature of the disease, the target antigen, possibly the affinity of the variant of the OB-fold protein against this antigen, weight of the patient, use in combination or not with other drugs for the pathology). The range will therefore generally range from 10 mg / kg to 200 mg / kg, or even 400 mg / kg of the variant of the fold-OB protein in one or more doses. However, and as stated above, these limit values are only indications, and it is possible to prepare compositions for administering more or less product.

The variant present in the composition according to the invention binds specifically to a target of interest. In fact, it may have been selected by a method as described in WO 2008/068637 or WO 2007/139397 for its binding specificity with this target of interest. Moreover, the methods described in these patent applications make it possible to obtain affinities of the order of one micromolar (WO 2007/139397) or nanomolar (WO 2008/068637).

The targets of interest are chosen according to the disease that one wishes to treat. Thus, any antigen, antibody, cellular protein, circulating protein, peptides may be mentioned. One can also target a drug active ingredient, or a particular nucleic acid. It is contemplated in particular that the target of interest is an interleukin, a cytokine, a cytokine or interleukin receptor, an oncogene encoded protein, a microorganism surface protein, or a microorganism lipopolysaccharide.

The composition according to the invention can be in any form known in the art. In particular, it is in the form of capsules, tablets (film-coated or not), pills or tablets. In another embodiment, it is in the form of a liquid composition, such as a syrup. It can also be in solid form,

In the case where the composition is in a solid form, any excipient known in the art, such as talc (E553b), microcrystalline cellulose, lactose, starch (in particular corn), magnesium stearate (E572), stearic acid (E570). microcrystalline cellulose. When the composition is in the form of a film-coated tablet, said film may be formed of any substance known in the art, such as hypromellose (E464), ethylcellulose, macrogol, Talc (E553b), titanium dioxide (E171), iron oxide (E172).

The compositions can also be delayed release (slow release). Such controlled or delayed release formulations are described, in particular, in WO 201 1/077239. Thus, these compositions may include matrices in which OB-fold proteins (natural or variants) are present, optionally with other ingredients. These matrices may be such that they allow immediate release of a portion of the OB fold proteins, followed by delayed release of another portion of these proteins.

In oral compositions in solid form, the proteins may be freeze-dried or integrated into templates as described in WO 98/043615.

It should be noted, however, that the examples show clearly that the variants of the fold-OB proteins, and in particular when the OB fold protein is the Sac7d family (SEQ ID No. 1 to SEQ ID No. 7) are resistant to gastric degradation and can therefore operate at the level of the intestine, or even the systemic circulation. It is therefore clear that even if the elements of the oral administration composition can improve the protection of these proteins, this is just a plus, but not an essential element in achieving the technical effect.

When the compositions are in liquid form, the proteins are generally present directly in the solution.

PBS (phosphate buffered saline, physiological saline containing sodium chloride, disodium phosphate, potassium dihydrogen phosphate and a little potassium chloride), TBS (Tris-buffered saline), buffer citrate (made especially with monosodium citrate, 100 mM), or HEPES (4- (2-hydroxyethyl) -1-piperazine ethane sulfonic acid, zwitterionic organic compound, buffer having good stability at physiological pH).

Apart from the citrate buffer for which the pH is adjusted between 4 and 6, the buffers are preferably at pH 7.4.

However, it is possible to use other types of buffers to prepare oral liquid compositions.

Of course, it is preferable that the preparation of these buffers is carried out under conditions allowing administration to patients (traceability, good manufacturing practices, etc.).

The variants of the fold-OB proteins used in the composition according to the invention can be produced by solid phase chemical synthesis or by genetic recombination. The chemical synthesis can be carried out for example with an automatic peptide synthesizer of the Applied Biosystems type, mod. 433A., Or in Fmoc chemistry which uses the fluoremylmethyloxycarbonyl group for the temporary protection of the α-amino function of the amino acids.

It is, however, preferred to produce the variants which can be used in the context of the invention by genetic engineering, in particular by integrating a nucleic acid sequence coding for said polypeptide into an expression vector. This expression vector is then introduced into a host cell (bacteria such as Escherichia coli are particularly suitable), which is cultured under culture conditions for the synthesis of the polypeptide (it is particularly possible to use inducible promoters upstream of the polypeptide in the expression vector. The synthesized polypeptide is then recovered. We can then graft any type of N- or C-terminal molecules of the polypeptide.

Those skilled in the art are familiar with methods for producing polypeptides, which are described in particular in Sambrook, Fritsch and Maniatis, MOLECULAR CLONING, A LABORATORY MANUAL, 2nd edition.

The composition according to the invention may contain variants of the fold-OB protein alone or with other active ingredients. Thus, the composition may also contain at least one agent chosen from antibacterial, antiparasitic, antifungal, anti-inflammatory, antipruritic, anesthetic, antiviral, keratolytic and anti-free radical agents.

This composition may also contain a pH regulating agent, in particular to allow the regulation of the pH around pH 7.

The variants of the fold-OB protein may also be fused with an active protein or any other compound, in particular in order to increase their half-life time.

The composition according to the invention can also be used in a diagnostic method. Thus, in a particular embodiment, the variant of the fold-OB protein is coupled to a detection or contrast agent, a tracer or a metal. This allows in particular a follow-up of this detection agent (contrast agent, tracer, metal) and to determine the organs on which the variant of the fold-OB protein binds (which indicates the presence of the target of interest) . The invention thus relates to a method for detecting the presence of a specific antigen in an organ, particularly in the gastrointestinal tract, comprising the step of administering an oral composition as described herein. above, said composition comprising a variant of a fold-OB protein binding to said antigen, and coupled to a detectable tracer (in particular the detection of emission of radiation emitted by the tracer, or a metal, or a contrast agent ). This method may also include the step of detecting the presence of the tracer in the human body, and locating the organ in which this tracer is detected, making it possible to conclude that the antigen is present. in the organ where this tracer is detected. This conclusion about the presence of the antigen in an organ is key to conclude this diagnostic method, because it allows to conclude as to the existence of a particular pathology, especially if the antigen is a marker of this pathology . The most common tracers are isotopes (half-life of less than two hours), such as fluorine 18 ( ¹⁸ F) or other radioelements such as ¹⁵ 0, ¹³ N and ¹¹ C.

The invention also relates to a method for preparing an orally administered composition, comprising the step of mixing a variant of a wild-fold OB-protein with a pharmaceutically acceptable excipient for oral administration.

The invention also relates to a composition for oral administration, according to the invention, containing a variant of a wild-type OB protein, said variant having between 5 and 32 mutated residues in the binding interface of said OB-fold wild-type protein to its natural ligand, as a drug. In this particular case, said variant specifically binds to a target of interest, which is a therapeutic target. The invention also relates to a composition for oral administration according to the invention for the treatment of a disease or a systemic disorder or more specifically of a disease or a disorder of the gastrointestinal system. In this embodiment, the variant of the fold-OB protein used targets (binds to) an etiological factor of the targeted disease or a therapeutic target linked to this disease.

A disease of the gastrointestinal system is a disease particularly chosen from amoebiasis, cancers of the colon and rectum, cancers of the stomach and duodenum, cancers of the esophagus, inflammatory diseases of the digestive system (IBD), cancer pancreas, cholera, hepatitis and cirrhosis of the liver (particularly hepatic due to B or C viruses), colitis (particularly due to Closrtidium), diarrhea (especially bacterial (especially Shigella, Campylobacter, Salmonella, Yersinia pseudotuberculosis and Yersinia enterocolitica) or viral (in particular due to parvovirus and reovirus, rotavirus (reo-like virus), enterovirus, astrovirus, corona-like virus), adult celiac disease, Whipple's disease, pancreatitis, irritable bowel syndrome, tumors abdominal, liver tumors, duodenum or stomach ulcer, intestinal worms, Zollinger and Ellison syndrome.

A systemic disease is a disease localized in an organ other than the gastrointestinal system.

In this embodiment, a variant of the fold-OB protein is therefore selected, in particular by the screening methods described in WO 2008/068637, which binds to a therapeutic target (effector or etiological factor) involved in the disease or the disorder that it is desired to treat, and this variant is formulated in a composition for oral administration.

The invention also relates to a method of treating a disease or a systemic disorder or more specifically a disease or a disorder of the gastrointestinal system, characterized in that it is administered orally a composition according to the invention containing a therapeutically effective amount of a binding-binding (binding to) OB protein, preferably an etiological factor or a therapeutic target characteristic of said disease or disorder.

Examples

In all of the examples, nanofitins, as defined above, that is to say Sac7d variants, obtained by screening a combinatorial library against a target of interest, using a similar method, are used. to the method described in WO 2008/068637. The purpose of these examples is to demonstrate that OB-fold proteins, and in particular nanofitins, are able to resist degradation in the stomach and have an effect directly on the site of the gastrointestinal system (intestine in example) where their action is necessary. Example 1 Efficacy Test of Nanofitins Administered by Oral View

Three nanofitins A1, A2, A3 from a library of Sac7d variants were tested for their affinity against a target of interest, implicated in a disease of the gastrointestinal system (inflammation of the intestine). These nanofitins were produced in a bacterial system, either in the form of a fusion with a polyhistin label, or in the absence of fusion (un-labeled). The nanofitins were suspended in PBS (phosphate buffered saline). These nanofitins were tested on a mouse model of intestinal inflammation (colitis) induced with TNBS (2,4,6-trinitrobenzenesulfonic acid), as described in Scheiffele and Fuss. (Curr Protoc Immunol, 2002 Aug; Chapter 15: Unit 15.19), either in preventive mode with the application of a dose of nanofitin per day starting 5 days before TNBS induction and a sacrifice of the mice 2 days later, or in curative mode with application of a dose of nanofitin per day from the day of TNBS induction and sacrifice of the mice 4 days later.

The effect of nanofitins has been evaluated at the macroscopic level and at the histological level. For macroscopic evaluation, the colon was examined under a dissection microscope (x5) to evaluate lesions according to Wallace criteria. Wallace's score evaluates macroscopic lesions on a scale of 0 to 10 based on criteria reflecting inflammation (0 corresponding to no inflammation and 10 to aggravated inflammation), such as hyperemia, number and the extent of ulcerations (Pierre Desreumaux, 2001, J Exp Med., 193, 827-838). For histological evaluation, a piece of colon located 2 cm above the anal canal was cut, then fixed overnight in 4% paraformaldehyde and embedded in paraffin. The sections labeled with hematoxylin and eosin were examined "blind" and evaluated according to the Ameho criteria. The Ameho score evaluates lesions on a scale of 0 to 6 based on criteria reflecting inflammation (0 corresponding to the absence of inflammation and 6 to aggravated inflammation) such as cell infiltration, depth and extension on the surface of the lesion (Pierre Desreumaux, 2001, J Exp Med., 193, 827-838). In both cases, the results were converted to percent efficiency reflecting the percentage decrease in score relative to the overall score of untreated induced mice.

As a control, a reference molecule marketed as intestinal anti-inflammatory drug, Pentasa® (5-amino-salicylic), used at its optimum dose was used. The results are given by way of reference only, as the dosages and route of administration are not strictly identical to those applied for nanofitins.

Applied preventively rectally (30 mM), Pentasa® gives an efficacy of 37% (macroscopic level) and 29% (histological level). Applied in the curative model (ad libitdum presence in animal feed), Pentasa® gives an efficacy of 59% (macroscopic level) and 39% (histological level).

H: histological efficacy

Table I - Results obtained on model of intestinal inflammation (percentage of effectiveness)

These results show that nanofitins are able to act directly on the localized target in the gut after oral administration, that they effectively pass through the stomach without being degraded, and that they have levels of effectiveness comparable with the reference product.

Claims

1. A composition for oral administration comprising a variant of a wild-fold OB protein, said variant having between 5 and 32 mutated residues in the binding interface of said wild-fold OB protein to its natural ligand.

2. Composition according to claim 1, characterized in that said wild-fold protein OB is selected from Sac7d or Sac7e from Sulfolobus acidocaldarius, Sso7d from Sulfolobus solfataricus, DBP 7 from Sulfolobus tokodaii, Ssh7b from Sulfolobus shibatae, Ssh7a from Sulfolobus shibatae, and p7ss from Sulfolobus solfataricus.

3. Composition according to one of claims 1 to 2, characterized in that said variant binds to a target of interest selected from antigens, antibodies, cellular proteins, circulating proteins, peptides, active principles of drugs, nucleic acids, and especially interleukins, cytokines, cytokine receptors or interleukins, proteins encoded by oncogenes, surface proteins of microorganisms, and lipopolysaccharides of microorganisms.

4. Composition according to one of claims 1 to 3, characterized in that it is in the form of capsules, tablets, tablets or pills.

5. Composition according to one of claims 1 to 3, characterized in that it is in the form of a liquid composition.

6. Composition according to one of claims 1 to 5, characterized in that it further contains at least one agent selected from antibacterial, antiparasitic, antifungal, anti-inflammatory, antipruriginous, anesthetic, antiviral, keratolytic, anti- free radicals.

7. Composition according to one of claims 1 to 6 for its use in the treatment of a disorder or disease of the gastrointestinal system.

Process for the preparation of an oral composition according to one of claims 1 to 7, comprising the step of mixing a variant of a wild-fold protein OB, said variant exhibiting between 5 and 32 mutated residues in the binding interface of said wild-fold OB protein to its natural ligand to a pharmaceutically acceptable vehicle for oral administration.

A method for detecting the presence of a specific antigen in an organ, particularly in the gastrointestinal tract, comprising the step of administering to said patient a composition according to one of claims 1 to 6, said composition comprising a variant of a fold-OB protein binding to said desired antigen, and coupled to a tracer.